ID

26228

Beskrivning

Study ID: 100601 Clinical Study ID: LPL100601 Study Title: LPL100601, A Clinical Outcomes Study of Darapladib versus Placebo in Subjects with Chronic Coronary Heart Disease to Compare the Incidence of Major Adverse Cardiovascular Events (MACE) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00799903 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: darapladib Trade Name: darapladib Study Indication: Atherosclerosis Study part: End of study contact

Nyckelord

  1. 2017-10-12 2017-10-12 -
  2. 2017-10-13 2017-10-13 -
  3. 2017-10-23 2017-10-23 -
  4. 2018-01-02 2018-01-02 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

12 oktober 2017

DOI

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Licens

Creative Commons BY-NC 3.0

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End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

End of study contact form
Beskrivning

End of study contact form

1. Was subject contacted?
Beskrivning

subject contact

Datatyp

boolean

Type of contact
Beskrivning

Type of contact

Datatyp

integer

If telephone: Time of contact
Beskrivning

Time of contact

Datatyp

time

If telephone: Site staff who conducted call
Beskrivning

ensure documented in source notes

Datatyp

text

If telephone: Reason why visit was not perfomed in the clinic
Beskrivning

Reason visit was not perfomed in clinic

Datatyp

text

Other, specify
Beskrivning

Reason visit was not perfomed in clinic specification

Datatyp

text

Similar models

End of study contact GSK study Chronic Coronary Heart Disease NCT00799903

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
End of study contact form
subject contact
Item
1. Was subject contacted?
boolean
Item
Type of contact
integer
Code List
Type of contact
CL Item
Clinic visit (1)
CL Item
Telephone (2)
Time of contact
Item
If telephone: Time of contact
time
Item
If telephone: Site staff who conducted call
text
Code List
If telephone: Site staff who conducted call
CL Item
Physician (34)
CL Item
Nurse (35)
CL Item
Other (OT)
Item
If telephone: Reason why visit was not perfomed in the clinic
text
Code List
If telephone: Reason why visit was not perfomed in the clinic
CL Item
Subject refused (1)
CL Item
Subject not able to visit clinic (2)
CL Item
Other (OT)
Reason visit was not perfomed in clinic specification
Item
Other, specify
text

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